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Accueil du site > Recherche > Dauban P. > Publications par thèmes

Publications par thèmes

Revues sur la chimie des nitrènes :

  1. P. Dauban, R.H. Dodd "Iminoiodanes and C-N bond formation in organic synthesis" Synlett 2003, 1571-1586.
  2. Dauban, R.H. Dodd "Catalytic C-H Amination using Nitrenes" Amino Group Chemistry : From Synthesis to the Life Sciences, A. Ricci, Ed. ; Wiley-VCH, Weinheim, 2007, pp. 55-92.
  3. F. Collet, R.H. Dodd, P. Dauban "Catalytic C-H amination : recent progress and future directions." Chem. Commun. 2009, 5061-5074.
  4. F. Collet, C. Lescot, P. Dauban "Catalytic C-H amination : the stereoselectivity issue." Chem. Soc. Rev. 2011, 40, 1926-1936.

Nitrène et Amination C-H :

  1. C. Liang, F. Robert-Peillard, C. Fruit, P. Müller, R.H. Dodd, P. Dauban "Efficient diastereoselective intermolecular rhodium-catalyzed C-H amination." Angew. Chem. Int. Ed. 2006, 45, 4641-4644.
  2. C. Liang, F. Collet, F. Robert-Peillard, P. Müller, R.H. Dodd, P. Dauban "Toward a Synthetically Useful Stereoselective C-H Amination of Hydrocarbons." J. Am. Chem. Soc. 2008, 130, 343-350.
  3. F. Collet, C. Lescot, C. Liang, P. Dauban "Studies in catalytic C-H amination involving nitrene C-H insertion." Dalton Trans. 2010, 39, 10401-10413.
  4. C. Lescot, B. Darses, F. Collet, P. Retailleau, P. Dauban "Site-selective catalytic C-H amination." Chem. Eur. J. 2012, submitted

Nitrène et Aziridination :

Génération in situ de nitrène

  1. P. Dauban, L. Sanière, A. Tarrade, R.H. Dodd "Copper-catalyzed nitrogen transfer mediated by iodosylbenzene PhI=O." J. Am. Chem. Soc. 2001, 123, 7707-7708.

Génération à partir de sulfonamides

  1. P. Dauban, R.H. Dodd "PhI=NSes : A new iminoiodinane reagent for the copper-catalyzed aziridination of olefins." J. Org. Chem. 1999, 64, 5304-5307.
  2. P. Dauban, R.H. Dodd "Synthesis of cyclic sulfonamides via intramolecular copper-catalyzed reaction of unsaturated iminoiodinanes." Org. Lett. 2000, 2, 2327-2329.
  3. P. Dauban, R.H. Dodd "Intramolecular bromine-catalyzed aziridination : a new direct access to cyclic sulfonamides." Tetrahedron Lett. 2001, 42, 1037-1040.

Génération à partir de sulfamates

  1. F. Duran, L. Leman, A Ghini, G. Burton, P. Dauban, R.H. Dodd "Intramolecular PhI=O mediated copper-catalyzed aziridination of unsaturated sulfamates" Org. Lett. 2002, 4, 2481-2483.
  2. A. Estéoule, F. Duran, P. Retailleau, R.H. Dodd, P. Dauban "Enantioselective intramolecular copper-catalyzed aziridination of sulfamates." Synthesis 2007, 1251-1260.
  3. G. Malik, A. Estéoule, P. Retailleau, P. Dauban "Aziridine from intramolecular alkene aziridination of sulfamates : reactivity toward carbon nucleophiles. Application to the synthesis of Spisulosine and its fluoro analogue." J. Org. Chem. 2011, 76, 7438-7448.

Aziridination diastéréosélective

  1. P.H. Di Chenna, F. Robert-Peillard, P. Dauban, R.H. Dodd "Sulfonimidamides : efficient chiral iminoiodane precursors for diastereoselective copper-catalyzed aziridination of olefins." Org. Lett. 2004, 6, 4503-4505.
  2. C. Fruit, F. Robert-Peillard, G. Bernardinelli, P. Müller, R.H. Dodd, P. Dauban "Diastereoselective rhodium-catalyzed nitrene transfer starting from chiral sulfonimidamide-derived iminoiodanes." Tetrahedron : Asymmetry 2005, 16, 3484-3487.
  3. F. Robert-Peillard, P. H. Di Chenna, C. Liang, C. Lescot, F. Collet, R.H. Dodd, P. Dauban "Catalytic stereoselective alkene aziridination with sulfonimidamides." Tetrahedron : Asymmetry 2010, 21, 1447-1457

Quelques applications en synthèse et chimie médicinale

  1. L. Leman, L. Sanière, P. Dauban, R.H. Dodd "Copper-catalyzed aziridination of allylglycine derivatives" Arkivoc 2003, vi, 126-134.
  2. L. Sanière, L. Leman, J.J. Bourguignon, P. Dauban, R.H. Dodd "Iminoiodane mediated aziridination of α-allylglycine : access to a novel rigid arginine derivative and to the natural amino acid enduracididine." Tetrahedron 2004, 60, 5889-5897.
  3. F.J. Duran, A.A. Ghini, P. Dauban, R.H. Dodd, G. Burton "Synthesis of 6,19-sulfamidate bridged pregnanes." J. Org. Chem. 2005, 70, 8613-8616.
  4. A. Kessler, H. Faure, C. Petrel, D. Rognan, M. Césario, M. Ruat, P. Dauban, R.H. Dodd "N1-Benzoyl-N2-[1-(1-naphthyl)ethyl]-trans-1,2-diaminocyclohexanes : Development of Calhex 231 as a New Calcium Sensing Receptor (CaSR) Ligand Demonstrating Potent Calcilytic Activity." J. Med. Chem. 2006, 49, 5119-5128.
  5. F.J. Duran, V.C. Edelsztein, A.A. Ghini, M. Rey, H. Coirini, P. Dauban, R.H. Dodd, G. Burton "Synthesis and GABA-A receptor activity of 2,19-sulfamoyl analogues." Bioorg. Med. Chem. 2009, 17, 6526-6533.
  6. P. Dauban, G. Malik "A new masked 1,3-dipole revealed from aziridines." Angew. Chem. Int. Ed. 2009, 48, 9026-9029.

Nitrène et Oxyamination :

  1. S. Beaumont, V. Pons, P. Retailleau, R.H. Dodd, P. Dauban "Catalytic oxyamidation of indoles." Angew. Chem. Int. Ed. 2010, 49, 1634-1637.
  2. N. Gigant, G. Dequirez, P. Retailleau, I. Gillaizeau, P. Dauban "Catalytic selective oxyamidation of cyclic enamides using nitrenes" Chem. Eur. J. 2012, 18, 90-94.

Nitrène et Imination de sulfures :

  1. F. Collet, R.H. Dodd, P. Dauban "Stereoselective rhodium-catalyzed imination of sulfides." Org. Lett. 2008, 10, 5473-5476.

Articles sur invitation publiés dans e-EROS :

  1. P. Dauban, R.H. Dodd "[N-(2-(trimethylsilyl)ethanesulfonyl)imino]phenyliodane" 2003
  2. P. Dauban, R.H. Dodd "Copper(I) trifluoromethanesulfonate" 1st Update 2004
  3. V. Pons, R.H. Dodd, P. Dauban "Bis(2,2-dimethylpropanoato-κ-O)phenyl-Iodine" 2009
  4. B. Darses, P. Dauban "Iodosylbenzene" 3rd Update 2012

Cancer : méthodologies de synthèse et nouvelles molécules actives :

  1. L. Keller, S. Beaumont, J.-M. Liu, S. Thoret, J. Bignon, J. Wdzieczak-Bakala, P. Dauban, R.H. Dodd "New C5-alkylated indolobenzazepinones acting as inhibitors of tubulin polymerization : cytotoxic and antitumor activities." J. Med. Chem. 2008, 51, 3414-3421.
  2. S. Beaumont, P. Retailleau, P. Dauban, R.H. Dodd "Synthesis of indolobenzazepinones by application of an isocyanide-based multicomponent reaction." Eur. J. Org. Chem. 2008, 5162-5175.
  3. D. Gauthier, R.H. Dodd, P. Dauban "Regioselective access to substituted oxindoles via rhodium-catalyzed C-H insertion." Tetrahedron 2009, 65, 8542-8555.